T. Sugama et Rn. Mora, VINYLPHOSPHONIC ACID-MODIFIED CALCIUM ALUMINATE AND CALCIUM SILICATE CEMENTS, Journal of Materials Science, 31(23), 1996, pp. 6269-6278
Cementitious materials in terms of calcium phosphate cements (CPC) wer
e prepared through the acid-base reaction between vinylphosphonic acid
(VPA) and calcium aluminate cement (CAC) reactants or calcium silicat
e cement (CSC) reactants at 25 degrees C. Using CAC, two factors were
responsible for the development of strength in the cements: one is the
formation of an amorphous calcium-complexed vinylphosphonate (CCVP) s
alt phase as the reaction product, and the other was the high exotherm
ic reaction energy. Because the formation of CCVP depletes the calcium
in the CAC reactants, Al2O3 . xH(2)O gel was precipitated as a by-pro
duct. CCVP --> amorphous calcium pyrophosphate hydrate (CPPH) and Al2O
3 . xH(2)O --> gamma-AlOOH phase transitions occurred in the CPC body
autoclaved at 100 degrees C. Increasing the temperature to 200 degrees
C promoted the transformation of CPPH into crystalline hydroxyapatite
(HOAp). In the VPA-CSC system, the strong alkalinity of CSC reactant
with its high CaO content served in forming the CPPH reaction product
which led to a quick setting of the CPC at 25 degrees C. Hydrothermal
treatment at 100 degrees C resulted in the CPPH --> HOAp phase transit
ion, which was completed at 300 degrees C for both the VPA-CAC and VPA
-CSC systems, and also precipitated the silica gel as by-product. Alth
ough the porosity of the specimens was one of the important factors go
verning the improvement of strength, a moderately mixed phase of amorp
hous CPPH and crystalline HOAp as the matrix layers contributed signif
icantly to strengthening of the CPC specimens.